Spectral tuning of azobenzene photoswitches for biological applications

Angew Chem Int Ed Engl. 2009;48(8):1484-6. doi: 10.1002/anie.200805013.

Abstract

Longer switching wavelengths and good photochemical yields and stabilities of the cis isomers in reducing aqueous environments are achieved by introducing 2,2'-aminoalkyl substituents into 4,4'-diamido-substituted azobenzenes. The products are thus suitable for photocontrol of biomolecular structures in intracellular environments, such as switching between two peptide configurations (see picture).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Azo Compounds / chemical synthesis
  • Azo Compounds / chemistry*
  • Azo Compounds / radiation effects
  • Circular Dichroism
  • Peptides / chemistry
  • Spectrophotometry, Infrared
  • Spectrophotometry, Ultraviolet
  • Stereoisomerism

Substances

  • Azo Compounds
  • Peptides
  • azobenzene